Gene table: search width pubmed_id = 19251977


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital myasthenic syndrome with nephrotic syndrome - (AR)
11.34
19251977
LAMB2 (3p21)
Laminin, beta 2 (laminin S)
* Congenital myasthenic syndrome with nephrotic syndrome - NPHS5